Procollagen C-Proteinase Enhancer 1 (PCPE-1) as a Plasma Marker of Muscle and Liver Fibrosis in Mice

Autor: Mary Safrin, Eyal Hassoun, Hana Ziv, Sarah Pri-Chen, Efrat Kessler
Rok vydání: 2016
Předmět:
0301 basic medicine
Pathology
Physiology
Respiratory System
lcsh:Medicine
030204 cardiovascular system & hematology
Platelet membrane glycoprotein
Biochemistry
Basal (phylogenetics)
0302 clinical medicine
Fibrosis
Blood plasma
Thoracic Diaphragm
Medicine and Health Sciences
Enzyme-Linked Immunoassays
lcsh:Science
Multidisciplinary
medicine.diagnostic_test
Liver Diseases
Hematology
Animal Models
Body Fluids
Precipitation Techniques
Blood
Biomarker (medicine)
Liver Fibrosis
Anatomy
Type I collagen
Research Article
medicine.medical_specialty
Mouse Models
Gastroenterology and Hepatology
Biology
Immunofluorescence
Research and Analysis Methods
Blood Plasma
03 medical and health sciences
Model Organisms
medicine
Immunoprecipitation
Immunoassays
lcsh:R
Biology and Life Sciences
Proteins
Correction
medicine.disease
Procollagen peptidase
030104 developmental biology
Immunologic Techniques
lcsh:Q
Collagens
Developmental Biology
Zdroj: PLoS ONE
PLoS ONE, Vol 11, Iss 7, p e0159606 (2016)
ISSN: 1932-6203
Popis: Current non-invasive diagnostic methods of fibrosis are limited in their ability to identify early and intermediate stages of fibrosis and assess the efficacy of therapy. New biomarkers of fibrosis are therefore constantly sought for, leading us to evaluate procollagen C-proteinase enhancer 1 (PCPE-1), a fibrosis-related extracellular matrix glycoprotein, as a plasma marker of fibrosis. A sandwich ELISA that permitted accurate measurements of PCPE-1 concentrations in mouse plasma was established. Tissue fibrosis was assessed using histochemical, immunofluorescence, and immunoblotting analyses for type I collagen and PCPE-1. The normal plasma concentration of PCPE-1 in 6 weeks to 4 months old mice was ~200 ng/ml (189.5 ± 11.3 to 206.8 ± 13.8 ng/ml). PCPE-1 plasma concentrations in four and 8.5 months old mdx mice displaying fibrotic diaphragms increased 27 and 40% respectively relatively to age-matched control mice, an increase comparable to that of the N-propeptide of procollagen type III (PIIINP), a known blood marker of fibrosis. PCPE-1 plasma levels in mice with CCl4-induced liver fibrosis increased 34 to 50% relatively to respective controls and reflected the severity of the disease, namely increased gradually during the progression of fibrosis and went down to basal levels during recovery, in parallel to changes in the liver content of collagen I and PCPE-1. The results favor PCPE-1 as a potential new clinically valuable fibrosis biomarker.
Databáze: OpenAIRE